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New Ethylated Derivatives of Sulfur- and Nitrogen-Containing Artifacts from Tenodera sinensis Egg Pod and Their Anti-Renal Fibrosis
被引:0
|作者:
Chen, Ye-Fei
[1
,2
]
Peng, Shi-Gang
[1
,3
]
Yan, Yong-Ming
[1
]
Cheng, Yong-Xian
[1
,2
,3
]
机构:
[1] Shenzhen Univ, Inst Inheritance Based Innovat Chinese Med, Guangdong Key Lab Chinese Med Ingredients & Gut Mi, Marshall Lab Biomed Engn,Sch Pharm,Med Sch, Shenzhen 518055, Peoples R China
[2] Shenzhen Univ, Sch Biomed Engn, Natl Reg Key Technol Engn Lab Med Ultrasound, Guangdong Key Lab Biomed Measurements & Ultrasound, Shenzhen 518060, Peoples R China
[3] Chengdu Univ Tradit Chinese Med, Sch Pharm, Chengdu 611137, Peoples R China
来源:
关键词:
Mantidis ootheca;
Tenodera sinensis Saussure;
mantidisamides E-H;
renal fibrosis;
CHEMICAL-CONSTITUENTS;
POLYRHACHIS-DIVES;
FUNGUS;
METABOLITES;
D O I:
10.3390/molecules29153491
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Three pairs of enantiomers and one achiral molecule that are new ethylated derivatives of sulfur and nitrogen-containing compounds named mantidisamides E-H (1-4), along with twenty known ones (5-24), were derived from the ethanol extract of Tenodera sinensis Saussure. The structures of these new compounds and their absolute configurations were assigned on the basis of spectroscopic analyses and computational methods. The assessment of activities in NRK-52e cells induced by TGF-beta 1 demonstrated that the previously undescribed compounds 1 and 2 exhibited a significant capacity to inhibit the expression of proteins (fibronectin, collagen I, and alpha-SMA). Moreover, the biological activity of these compounds was found to increase with rising concentrations. Notably, compounds 1-4 should be artifacts; however, undescribed compounds 1 and 2, which possessed obvious biological activity, might be attractive for chemists and biologists due to the potential for more detailed exploration of their properties. It is worth mentioning that compounds 1 and 2 remain novel structures even in the absence of the ethoxy group.
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